M. Sato et al., Determination of aluminium in biological samples and drinking water by kinetic-differentiation mode HPLC with fluorescent detection, BUNSEKI KAG, 49(6), 2000, pp. 429-435
The development of a simple and sensitive method for the determination of a
luminium is a subject of growing interest. The objective of this study was
to apply kinetic-differentiation mode HPLC with 8-quinolinol to biological
and water samples. The aluminium chelate is detected fluorometrically at Ex
370 nm and Em 504 nm. The most remarkable point of the proposed method is
that only aluminium ion respond selectively among many metal ions in the sa
mple matrix. The limit of detection, 1 mu g/l, is approximately ten-times h
igher than that of graphite-furnace AAS, which is currently used in routine
work. Precautions to prevent aluminium contamination during sample prepara
tion are described. The proposed method has been successfully applied to se
rum, urine, tap water, and bottled mineral water. The most important practi
cal application is in the treatment of patients on dialysis for whom alumin
ium accumulation can present serious problems. A comparison of the aluminiu
m concentration between healthy subjects and subjects on dialysis has been
difficult because the concentrations in the former group approach the lower
limit of those detectable by conventional methods. Using the proposed HPLC
, it was determined that the average aluminium concentration in serum tvas
3 mu g/l for 240 healthy subjects, and 11 mu g/l for 196 patients on dialys
is.